FHIR IG analytics| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1251.29.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1251.29/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1251.29 |
| Version | 20231001 |
| Status | active |
| Date | 2023-10-01T01:01:17-04:00 |
| Name | ThyroidHormoneDisorder |
| Title | Thyroid Hormone Disorder |
| Realm | us |
| Authority | hl7 |
| Description | SNOMED CT intensional (rule-based) value set for defining thyroid hormone disorders, available for a range of potential uses including problem-oriented views of relevant clinical information, clinical decision support rules, electronic patient registries, and data analytics. |
| Purpose | (Clinical Focus: Broad group of diagnosis concepts for thyroid hormone disorders.),(Data Element Scope: Employs SNOMED CT concept hierarchies primarily in the Disorder (Clinical finding) branch, though some can be in the Situation with Explicit Context branch or the Procedure branch.),(Inclusion Criteria: Includes hyperthyroidism, hypothyroidism, thyroiditis, sick-euthyroid syndrome, and abnormal thyroid function laboratory tests.),(Exclusion Criteria: Does not automatically include thyroid cancers or nodules without a concomitant thyroid hormone abnormality.) |
No resources found
| CodeSystem | |
| sct | SNOMED codes used in this IG |
No narrative content found in resource
FHIR
FHIRsmith{
"resourceType": "ValueSet",
"id": "2.16.840.1.113762.1.4.1251.29",
"meta": {
"versionId": "8",
"lastUpdated": "2023-12-21T17:43:03.000-05:00",
"profile": [
"http://hl7.org/fhir/StructureDefinition/shareablevalueset",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
]
},
"extension": [
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueContactDetail": {
"name": "UTSW Clinical Informatics Center Author"
}
},
{
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2023-10-01"
},
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate": "2023-10-01"
}
],
"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1251.29",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113762.1.4.1251.29"
}
],
"version": "20231001",
"name": "ThyroidHormoneDisorder",
"title": "Thyroid Hormone Disorder",
"status": "active",
"date": "2023-10-01T01:01:17-04:00",
"publisher": "UTSW Clinical Informatics Center Steward",
"description": "SNOMED CT intensional (rule-based) value set for defining thyroid hormone disorders, available for a range of potential uses including problem-oriented views of relevant clinical information, clinical decision support rules, electronic patient registries, and data analytics.",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
"purpose": "(Clinical Focus: Broad group of diagnosis concepts for thyroid hormone disorders.),(Data Element Scope: Employs SNOMED CT concept hierarchies primarily in the Disorder (Clinical finding) branch, though some can be in the Situation with Explicit Context branch or the Procedure branch.),(Inclusion Criteria: Includes hyperthyroidism, hypothyroidism, thyroiditis, sick-euthyroid syndrome, and abnormal thyroid function laboratory tests.),(Exclusion Criteria: Does not automatically include thyroid cancers or nodules without a concomitant thyroid hormone abnormality.)",
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "237504004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "123766008"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "32454003"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "3716002"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "34486009"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "367524008"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "40930008"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "36985004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "237562002"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "276564000"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "237542005"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "190309006"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "59136001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "264580006"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "237543000"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "82119001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "90739004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "70953003"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "166345007"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "312399001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "131089005"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "131090001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "166331001"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "309080005"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "131017004"
}
]
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"filter": [
{
"property": "concept",
"op": "is-a",
"value": "166337002"
}
]
}
]
},
"expansion": {
"identifier": "urn:uuid:3f3b59ee-e1e3-4352-b86b-82ca1eb00f10",
"timestamp": "2025-05-23T21:00:27-04:00",
"total": 334,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "102871000119101",
"display": "Hypothyroidism due to thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "106451000119106",
"display": "Goiter due to thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10718002",
"display": "Juvenile myxedema (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10753681000119101",
"display": "Postpartum hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10754921000119106",
"display": "Hyperthyroidism in childbirth (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10754961000119101",
"display": "Postpartum hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10757711000119106",
"display": "Postpartum thyroid disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10760001000119100",
"display": "Thyroid disease in mother complicating childbirth (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10760041000119103",
"display": "Thyroiditis in mother complicating childbirth (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10760381000119106",
"display": "Thyroiditis in pregnancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10809101000119109",
"display": "Hypothyroidism in childbirth (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "111566002",
"display": "Acquired hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "111567006",
"display": "Refetoff syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1137378008",
"display": "Hypothyroidism due to and following radiotherapy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1142106007",
"display": "Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1153576003",
"display": "Serum thyroid stimulating hormone above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1153577007",
"display": "Serum thyroid stimulating hormone below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1156181008",
"display": "Adrenocorticotropic hormone resistance syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163019009",
"display": "Diffuse endemic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163093006",
"display": "Acute thyroiditis caused by fungus (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163095004",
"display": "Acute thyroiditis caused by bacterium (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1163454006",
"display": "Thyrotoxicosis due to hyperfunctioning follicular adenoma of thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1169369000",
"display": "Serum T4 below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1169370004",
"display": "Serum T4 above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1169371000",
"display": "T3 uptake above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1169372007",
"display": "T3 uptake below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179381000",
"display": "Acquired central hypothyroidism due to Sheehan syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179382007",
"display": "Acquired central hypothyroidism due to disorder of pituitary gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179384008",
"display": "Acquired central hypothyroidism caused by ionizing radiation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179385009",
"display": "Acquired central hypothyroidism caused by drug (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179392004",
"display": "Acquired central hypothyroidism due to traumatic injury (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179394003",
"display": "Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179395002",
"display": "Consumptive hypothyroidism caused by type 3 iodothyronine deiodinase (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179396001",
"display": "Congenital hypothyroidism due to thyroid deiodinase mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179397005",
"display": "Congenital hypothyroidism due to symporter mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179399008",
"display": "Congenital hypothyroidism due to thyroglobulin mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179400001",
"display": "Congenital hypothyroidism due to dual oxidase maturation factor 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179401002",
"display": "Congenital hypothyroidism due to peripheral resistance to thyroid hormone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1179404005",
"display": "Congenital hypothyroidism due to congenital anomaly of thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1186604007",
"display": "Abnormal thyroid function test caused by substance (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1186851006",
"display": "Thyroiditis caused by radiation due to and following iodine 131 treatment (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1186937007",
"display": "Abnormal thyroid function test due to assay interference (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1230272009",
"display": "Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "123766008",
"display": "Complex thyroid endocrine disorder (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124029003",
"display": "Protein-bound iodine above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "124030008",
"display": "Protein-bound iodine below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259591007",
"display": "Dementia due to acquired hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260240000",
"display": "Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1260241001",
"display": "Resistance to thyroid hormone due to mutation in thyroid hormone receptor beta (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1264402008",
"display": "Hypothyroidism due to systemic sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1279836009",
"display": "Familial multinodular goiter syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1281843005",
"display": "Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131017004",
"display": "Thyroid stimulating hormone level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131089005",
"display": "Thyroid hormone level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131090001",
"display": "Thyroid hormone level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131092009",
"display": "Thyroxine level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131093004",
"display": "Thyroxine level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131095006",
"display": "Triiodothyronine level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131096007",
"display": "Triiodothyronine level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131098008",
"display": "3,3'-diiodothyronine level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "131099000",
"display": "3,3'-diiodothyronine level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1351676004",
"display": "Goiter concurrent with and due to chronic lymphocytic inflammation of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1351677008",
"display": "Atrophy of thyroid concurrent with and due to chronic lymphocytic inflammation of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "137421000119106",
"display": "Graves' disease in remission (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "13795004",
"display": "Neonatal thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "14779006",
"display": "Hypothyroidism following external radiotherapy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15470004",
"display": "Toxic diffuse goiter with acropachy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166326003",
"display": "Serum T3 level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166327007",
"display": "Serum T3 level below reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166331001",
"display": "Serum thyroxine level outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166337002",
"display": "Serum thyroid stimulating hormone level outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166342005",
"display": "Triiodothyronine uptake test outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "166345007",
"display": "Thyroid hormone tests outside reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1740001000004102",
"display": "Iatrogenic thyrotoxicosis factitia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "17885001",
"display": "Iodotyrosine deiodination defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "18621008",
"display": "Transient decreased production of T>4< (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190236006",
"display": "Non-toxic nodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190237002",
"display": "Non-toxic uninodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190241003",
"display": "Toxic diffuse goiter with no crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190242005",
"display": "Toxic diffuse goiter with crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190244006",
"display": "Toxic uninodular goiter with no crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190247004",
"display": "Toxic multinodular goiter with no crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190255006",
"display": "Thyrotoxicosis due to ectopic thyroid nodule with no crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190256007",
"display": "Thyrotoxicosis due to ectopic thyroid nodule with crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190268003",
"display": "Congenital hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190277005",
"display": "Hypothyroidism caused by radiation (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190279008",
"display": "Iodine hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190282003",
"display": "Hypothyroidism resulting from para-aminosalicylic acid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190283008",
"display": "Hypothyroidism resulting from phenylbutazone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190284002",
"display": "Hypothyroidism caused by resorcinol (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190293001",
"display": "Acute thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190294007",
"display": "Acute non-suppurative thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190304001",
"display": "Dyshormonogenic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190308003",
"display": "Thyroid-binding globulin abnormality (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "190309006",
"display": "Thyroid atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "199235001",
"display": "Thyroid dysfunction during pregnancy, childbirth and the puerperium (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "206457007",
"display": "Neonatal jaundice with congenital hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "21279007",
"display": "Lingual thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "21367009",
"display": "Autosomal dominant variant form of albumin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "215677009",
"display": "Congenital hypothyroidism with ectopic thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "216693007",
"display": "Hypothyroid dwarfism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "217710005",
"display": "Congenital iodine deficiency syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "21983002",
"display": "Hashimoto thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "22350004",
"display": "T>3< thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "2241003",
"display": "X-linked absence of thyroxine-binding globulin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "22558005",
"display": "Iodide transport defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "23536000",
"display": "Iodotyrosyl coupling defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237494009",
"display": "Diffuse goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237498007",
"display": "Toxic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237499004",
"display": "Thyrotoxicosis due to Graves' disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237500008",
"display": "Hashitoxicosis - transient (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237501007",
"display": "Thyrotoxicosis due to acute thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237503005",
"display": "Borderline thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237504004",
"display": "Autonomous thyroid function (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237505003",
"display": "Apathetic thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237506002",
"display": "Thyrotoxicosis in pregnancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237507006",
"display": "Human chorionic gonadotrophin-induced thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237508001",
"display": "Iatrogenic thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237509009",
"display": "Thyrotoxicosis on thyroxine therapy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237510004",
"display": "Iodine-induced thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237512007",
"display": "Thyrotoxicosis due to thyrotropin-secreting pituitary adenoma (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237515009",
"display": "Congenital hypothyroidism without goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237516005",
"display": "Congenital thyroid hypoplasia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237517001",
"display": "Congenital atrophy of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237518006",
"display": "Hypothyroid goiter, acquired (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237519003",
"display": "Autoimmune hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237520009",
"display": "Hypothyroidism due to Hashimoto's thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237521008",
"display": "Hypothyroidism due to thyroid stimulating hormone receptor blocking antibody (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237526003",
"display": "Euthyroid with thyroid antibodies (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237527007",
"display": "Postablative hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237528002",
"display": "Post-infectious hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237529005",
"display": "Acute viral thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237538007",
"display": "Chronic thyroiditis with transient thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237539004",
"display": "Drug-induced thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237541003",
"display": "Silent thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237542005",
"display": "Sick-euthyroid syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237543000",
"display": "Thyroid hormone binding abnormality (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237544006",
"display": "Thyroid-binding globulin deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237545007",
"display": "Drug interference with thyroid-binding globulin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237546008",
"display": "Thyroid-binding globulin high (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237547004",
"display": "Familial dysalbuminemic hyperthyroxinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237548009",
"display": "Thyroid pre-albumin binding abnormality (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237549001",
"display": "Dysprealbuminemic euthyroidal hyperthyroxinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237550001",
"display": "Euthyroid hypothyroxinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237551002",
"display": "Euthyroid hyperthyroxinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237554005",
"display": "Familial dyshormonogenetic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237555006",
"display": "Hypothyroidism due to iodide trapping defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237556007",
"display": "Hypothyroidism due to iodide organification defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237558008",
"display": "Acquired atrophy of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237559000",
"display": "Thyroid hormone resistance syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237560005",
"display": "Generalized thyroid hormone resistance (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237562002",
"display": "Iodine deficiency syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237565000",
"display": "Congenital iodine deficiency syndrome of mixed type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237566004",
"display": "Congenital iodine deficiency syndrome of neurological type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237567008",
"display": "Subclinical iodine deficiency hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237569006",
"display": "Uninodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237570007",
"display": "Multinodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237571006",
"display": "Iodine-deficiency-related multinodular endemic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237695004",
"display": "Idiopathic thyroid stimulating hormone deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "237824009",
"display": "Juvenile Graves' disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "25008002",
"display": "Hyperthyroidism due to struma ovarii (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "25476006",
"display": "Acute suppurative thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "26151008",
"display": "Graves' disease with acropachy AND with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "26389007",
"display": "Toxic multinodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "264580006",
"display": "Thyroid dysfunction (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "26692000",
"display": "Central hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267369002",
"display": "Simple goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "267374005",
"display": "Toxic diffuse goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "268302006",
"display": "Aberrant thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "27059002",
"display": "Postoperative hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "274120003",
"display": "Thyroid disease in pregnancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "27538003",
"display": "Hyperthyroidism with Hashimoto disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "276564000",
"display": "Perinatal thyroid disorder of fetus and/or neonate (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "276565004",
"display": "Neonatal goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "276566003",
"display": "Transient neonatal hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "276629001",
"display": "Transient hypothyroxinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "276630006",
"display": "Transient hypothyrotropinemia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "278503003",
"display": "Congenital hypothyroidism with diffuse goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "286909009",
"display": "Thyrotoxicosis with or without goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "29028009",
"display": "Thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "2917005",
"display": "Transient hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "297267009",
"display": "Retrosternal thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "30229009",
"display": "Hypothyroidism due to infiltrative disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "309080005",
"display": "Thyroid stimulating hormone level above reference range (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "30985009",
"display": "Toxic nodular goiter with thyrotoxic storm (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "312399001",
"display": "Thyroid function tests abnormal (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "32454003",
"display": "Congenital anomaly of the thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "34486009",
"display": "Hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "3511005",
"display": "Infectious thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "353295004",
"display": "Graves' disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "360348000",
"display": "Pituitary thyroid hormone resistance (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "360353005",
"display": "Thyrotoxicosis due to pituitary thyroid hormone resistance (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "360358001",
"display": "Thyrotoxicosis due to overproduction of thyroid stimulating hormone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "360361000",
"display": "Thyrotoxicosis due to inappropriate thyroid stimulating hormone secretion (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "361125005",
"display": "Subacute autoimmune thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "361126006",
"display": "Subacute lymphocytic thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "361127002",
"display": "Atypical subacute thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "36241006",
"display": "Non-toxic multinodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "36641000119106",
"display": "Euthyroid thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "367201000119101",
"display": "Thyroiditis caused by amiodarone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "367524008",
"display": "Hypoplasia of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "367631000119105",
"display": "Hypothyroidism caused by drug (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "367741000119106",
"display": "Diffuse thyroid goiter without thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "368361000119108",
"display": "Thyrotoxicosis factitia without thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "369091000119106",
"display": "Hypothyroidism caused by amiodarone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "36985004",
"display": "Inherited disorder of thyroid metabolism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "3716002",
"display": "Goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "37429009",
"display": "Hypothalamic hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "38727009",
"display": "Subacute thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "39444001",
"display": "Hypothyroidism due to fibrous invasive thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "40539002",
"display": "Hypothyroidism following radioiodine therapy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "405629002",
"display": "Infant hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "405630007",
"display": "Infant hypothyroidism to 24 months of age (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "40607004",
"display": "Hyperthyroidism due to hydatidiform mole with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "40930008",
"display": "Hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "41300001",
"display": "X-linked reduction of thyroxine-binding globulin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "419153005",
"display": "Nodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "42277004",
"display": "Transient decreased production of T>3< (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "42785009",
"display": "Hypothyroidism due to cystinosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "427970008",
"display": "Subclinical hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "428041004",
"display": "Subacute granulomatous thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "428165003",
"display": "Hypothyroidism in pregnancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "43153006",
"display": "Myxedema (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "43449002",
"display": "Thyroglobulin proteolysis defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "43507005",
"display": "Adult myxedema (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "440092001",
"display": "Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "445878006",
"display": "Multifocal granulomatous folliculitis of the thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "44744000",
"display": "Hyperthyroidism due to molar thyrotropin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "45053005",
"display": "Chronic thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "45414006",
"display": "Glucocorticoid deficiency with achalasia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "45476004",
"display": "Iodine deficiency disease, non goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "4641009",
"display": "Myxedema heart disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "47378001",
"display": "Viral thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "479003",
"display": "Graves' disease with pretibial myxedema AND with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "49830003",
"display": "Hypothyroidism caused by food stuff (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "4997005",
"display": "Thyrotoxicosis factitia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "50375007",
"display": "Thyroid hormone responsiveness defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "52724003",
"display": "Iodide oxidation defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "52772002",
"display": "Postpartum thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "54823002",
"display": "Subclinical hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "55296004",
"display": "X-linked excess of thyroxine-binding globulin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "55838005",
"display": "Athyrotic hypothyroidism sequence (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "5604000",
"display": "Neonatal transient hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "56041007",
"display": "Hypothyroidism due to defect in thyroid hormone synthesis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "56112001",
"display": "Thyroxine transport defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "56805008",
"display": "Endemic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "56823000",
"display": "Cervical thyroid remnant (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "57185003",
"display": "Primary hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "57777000",
"display": "Toxic nodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "5834008",
"display": "Hyperthyroidism caused by potassium iodide (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "59136001",
"display": "Thyroid disease in mother complicating pregnancy, childbirth AND/OR puerperium (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "59957008",
"display": "Neonatal Graves' disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "60216004",
"display": "Toxic diffuse goiter with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "60268006",
"display": "Toxic diffuse goiter with pretibial myxedema (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "60733007",
"display": "Hypothyroidism due to amyloidosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "60968001",
"display": "Adenomatous goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "61037007",
"display": "Colloid goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "61556008",
"display": "Iatrogenic thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "62052002",
"display": "Hyperthyroidism caused by amiodarone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "62278002",
"display": "Toxic multinodular goiter with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "63115005",
"display": "Hypothyroidism due to scleroderma (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "63127008",
"display": "Thyroglobulin synthesis defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "64491003",
"display": "Myxedematous form of cretinism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "65237009",
"display": "Accessory thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "66185005",
"display": "Autosomal dominant excess of transthyretin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "66392007",
"display": "Substernal goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "66944004",
"display": "Autoimmune thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "67723002",
"display": "Hyperthyroidism caused by radio contrast dye (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "67761000119108",
"display": "Autonomously functioning thyroid goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "69329005",
"display": "Toxic uninodular goiter with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "698577000",
"display": "Infant hypothyroidism caused by maternal drug (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "699298009",
"display": "Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "70225006",
"display": "Hypothyroidism caused by iodide excess (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "702327009",
"display": "Monocarboxylate transporter 8 deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "703309000",
"display": "Familial gestational hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "70348004",
"display": "Pendred's syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "709124008",
"display": "Chronic fibrous thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "70953003",
"display": "Transient decreased production of thyroid hormone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "711518002",
"display": "Diffuse hyperplastic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "715734006",
"display": "Congenital absence of half of thyroid (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "716338001",
"display": "Muscular pseudohypertrophy and hypothyroidism syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "716743006",
"display": "Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717333002",
"display": "Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717334008",
"display": "Idiopathic congenital hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "718183003",
"display": "Familial thyroid dyshormonogenesis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "718193005",
"display": "Peripheral resistance to thyroid hormone (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "718194004",
"display": "Hypothyroidism due to mutation in transcription factor of pituitary development (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "718690009",
"display": "Congenital hypothyroidism due to absence of thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "72071001",
"display": "Mumps thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722051004",
"display": "Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722375007",
"display": "Bamforth Lazarus syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "72271000119100",
"display": "Hyperthyroidism in pregnancy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722938007",
"display": "Congenital central hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722939004",
"display": "Congenital hypothyroidism due to iodine deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722940002",
"display": "Acquired central hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722941003",
"display": "Secondary hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722942005",
"display": "Familial hyperthyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723409007",
"display": "Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "725462002",
"display": "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "73068003",
"display": "X-linked variant form of thyroxine-binding globulin (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "73869005",
"display": "Toxic uninodular goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "75065003",
"display": "Endemic cretinism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "75667007",
"display": "Lingual goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763890006",
"display": "Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "765326001",
"display": "Familial glucocorticoid deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770631009",
"display": "Genetic transient congenital hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771271000",
"display": "Steroid-responsive encephalopathy associated with autoimmune thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771510006",
"display": "X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "773987000",
"display": "Transient neonatal hypothyroidism due to neonatal iodine exposure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783177006",
"display": "Congenital hypothyroidism due to maternal intake of antithyroid drug (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "78574007",
"display": "Hypothyroidism due to sarcoidosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "79488001",
"display": "Thyroxine plasma membrane transport defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "80304004",
"display": "Intrathyroidal calcification AND goiter syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "81873006",
"display": "Iodide peroxidase defect (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "82119001",
"display": "Thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "82598004",
"display": "Secondary hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "83664006",
"display": "Idiopathic atrophic hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "83986005",
"display": "Severe hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "84362007",
"display": "Fibrous autoimmune thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "84781002",
"display": "Sporadic cretinism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "85568000",
"display": "Sporadic goiter (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "87232008",
"display": "Hyperthyroidism due to ectopic thyroid nodule (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "88104005",
"display": "Focal thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "88273006",
"display": "Iatrogenic hypothyroidism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "8868001",
"display": "Dyshormonogenetic goiter AND iodide leak (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "88740003",
"display": "Thyrotoxicosis factitia with thyrotoxic crisis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "89024000",
"display": "Riedel's thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "89261000",
"display": "Isolated thyrotropin deficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "89719007",
"display": "Thyrotoxicosis without goiter or other cause (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "90441002",
"display": "Chronic nonsuppurative thyroiditis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "90739004",
"display": "Thyrotoxicosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "92978002",
"display": "Congenital absence of thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "93359004",
"display": "Congenital malposition of the thyroid gland (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "9476000",
"display": "Chronic suppurative thyroiditis (disorder)"
}
]
}
}